Human Phenotype Ontology 
Grandparent Node:
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Syndactyly (HP:0001159)help
Parent Node:
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Finger syndactyly (HP:0006101)help
..Starting node
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4-5 finger syndactyly (HP:0010705)help
Term ID: 10705
Name: 4-5 finger syndactyly
Synonym: Webbed 4th-5th finger
Definition: Syndactyly with fusion of fingers four and five.
Comments:
Reference: HP:0010705
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 finger syndactyly (HP:0010704) help
..expand1-3 finger syndactyly (HP:0010706) help
..expand1-4 finger syndactyly (HP:0010707) help
..expand1-5 finger syndactyly (HP:0010708) help
..expand2-3 finger syndactyly (HP:0001233) help
..expand2-4 finger syndactyly (HP:0010709) help
..expand2-5 finger syndactyly (HP:0010692) help
..expand3-4 finger syndactyly (HP:0006097) help
..expand3-5 finger syndactyly (HP:0010710) help
..expandCutaneous finger syndactyly (HP:0010554) help
..expandOsseous finger syndactyly (HP:0010492) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010705HP:00107054-5 finger syndactyly0DSP CL E G H18323052ORPHA:158687Lethal acantholytic erosive disorderHP:0040283 - Occasional747
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H26974274OMIM:164200Oculodentodigital dysplasia.68
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H26974274OMIM:257850Oculodentodigital dysplasia, autosomal recessive.68
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H26974274OMIM:186100Syndactyly, type III.68
HP:0010705HP:00107054-5 finger syndactyly0JUP CL E G H37286207ORPHA:158687Lethal acantholytic erosive disorderHP:0040283 - Occasional222
HP:0010705HP:00107054-5 finger syndactyly0RTTN CL E G H2591418654ORPHA:468631Microcephalic cortical malformations-short stature due to RTTN deficiencyHP:0040283 - Occasional113


Genes (4) :DSP GJA1 JUP RTTN

Diseases (5) :ORPHA:158687 OMIM:164200 OMIM:257850 OMIM:186100 ORPHA:468631
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.